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Réponses pour «proteomics»:

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201700000910 Gilquin B 100%

Proteomics 17, 1–2, 2017, 1600357 (1 of 5) 1600357 DOI 10.1002/pmic.201600357 TECHNICAL BRIEF A proteomics assay to detect eight CBRN-relevant toxins in food Benoit Gilquin1,2,3,4 , Michel Jaquinod1,2,3 , Mathilde Louwagie1,2,3 , Sylvie Kieffer-Jaquinod1,2,3 , Alexandra Kraut1,2,3 , Myriam Ferro1,2,3 , Franc¸ois Becher5 and Virginie Brun1,2,3 1 Universite´ Grenoble-Alpes, Grenoble, France CEA, BIG, Biologie a` Grande Echelle, Grenoble, France 3 INSERM, U1038, Grenoble, France 4 CEA, LETI, Clinatec, Grenoble, France 5 ´ ´ CEA, iBiTec-S, Laboratoire d’Etude du Metabolisme des Medicaments, Gif-sur-Yvette, France 2 A proteomics assay was set up to analyze food substrates for eight toxins of the CBRN (chemical, biological, radiological and nuclear) threat, namely ricin, Clostridium perfringens epsilon toxin (ETX), Staphylococcus aureus enterotoxins (SEA, SEB and SED), shigatoxins from Shigella dysenteriae and entero-hemorragic Escherichia coli strains (STX1 and STX2) and Campylobacter jejuni cytolethal distending toxin (CDT).


Matrigel 95%

1886 DOI 10.1002/pmic.200900758 Proteomics 2010, 10, 1886–1890 TECHNICAL BRIEF Matrigel:


201700000916 Gilquin B 94% Multiplex and accurate quantification of acute kidney injury biomarker candidates in urine using Protein Standard Absolute Quantification (PSAQ) and targeted proteomics MARK Benoît Gilquina,b,c, Mathilde Louwagiea,b,c, Michel Jaquinoda,b,c, Alexandre Cezd, Guillaume Picarda,b,c, Leila El Kholya,b,c, Brigitte Surine, Jérôme Garina,b,c, Myriam Ferroa,b,c, Thomas Kofmanf, Caroline Baraug, Emmanuelle Plaisierd,e,h, Pierre Roncod,e,h, ⁎ Virginie Bruna,b,c, a Université Grenoble-Alpes, F-38000 Grenoble, France CEA, BIG, Biologie à Grande Echelle, F-38054 Grenoble, France INSERM, U1038, F-38054 Grenoble, France d AP-HP, Hôpital Tenon, Department of Nephrology and Dialysis, F-75020 Paris, France e INSERM, UMR_S 1155, F-75005 Paris, France f AP-HP, Hôpital Henri Mondor, Department of Nephrology, F-94010 Créteil, France g AP-HP, Hôpital Henri Mondor, Plateforme de Ressources Biologiques, F-94010 Créteil, France h Sorbonne Universités, UPMC Univ Paris 06, UMR_S 1155, F-75005 Paris, France b c A R T I C L E I N F O A BS T RAC T Keywords:


grimplet 83%

Abstract In order to improve apricot (Prunus armeniaca) quality with markers assisted selection, 71 molecular markers involved in hormonal regulation and control of acidity and sugar content, texture, flavours and pigments biosynthesis were highlighted by transcriptomics and proteomics comparison of ripening stages and contrasted genotypes.


En Prospectus JIBioinfo2019 UMBB 68%

Thanks to advances in high throughput techniques and in information technologies, the omics sciences, including genomics, proteomics, transcriptomics and metabolomics, are today a major challenge in the identification and development of new diagnostic strategies, new markers and new biological targets, to better identify biological systems.


Postdoc InstitutCurie BioCell 2017 64%

quantitative live cell imaging on a newly acquired lattice light sheet microscope in combination with lipidomics and proteomics on purified uptake carriers.


Ad 64%

Candidates with previous experience with fly handling, NGS analysis and/or proteomics are particularly encouraged to apply.


Post doc EMBL Rome RM 00067 63%

Postdoctoral Fellow Location: Staff Category:



Therefore, the proteomics approach indeed identified specific components of an Orb2 protein complex in the adult Drosophila brain.


Postdoc eq Soler Chromatin Looping1 63%

We are looking for a highly motivated postdoctoral fellow to (i) identify regulatory factors involved in chromatin loop formation and modulation, and (ii) functionally characterize such factors using proteomics and functional genomics tools.


postdoctoral position 62%

protein biochemistry, proteomics, protein-protein interactions, protein covalent modification, site-directed mutagenesis, protein expression, mass spectrometry and bioinformatics is highly desirable.


report danger des champs bioinitiative 56%

Release Date: August 31, 2007 BioInitiative Report:


Interchim Blog Halo2 Flyer ITM 0914 54%

Sub-2 µm Non-core UHPLC Columns · Fused-Core UHPLC columns with ~300K plates per meter - Higher efficiency than existing non-core sub-2 µm columns · Longer column lifetime – more injections, less downtime - Due to Fused-Core 2 micron particle architecture, 1 micron frits can be used on the column inlet - 1 micron frits are less likely to be plugged by UHPLC samples or mobile phase contaminants than typical 0.2 – 0.5 µm frits on sub-2 µm non-core columns · All of the advantages of sub-2 µm non-core particles at lower operating pressures - High speed and efficiency with short columns - Improved productivity from faster analyses - Less solvent usage from shorter analysis times - High resolution and peak capacity in longer columns - Sharper, taller peaks = better sensitivity and lower LOD and LOQ - Lower back pressure than most commercially available non-core sub-2 µm columns HALO Fused-Core Columns Have Revolutionized HPLC and now UHPLC Separations 2006 HALO 2.7 micron Fused-Core columns introduced for HPLC and UHPLC separations – deliver similar efficiency to sub-2 µm non-core columns 2012 HALO 5 micron Fused-Core columns introduced to replace underperforming non-core HPLC columns to advance lower pressure HPLC applications sub-2 µm Non-core UHPLC Columns 1.7 µm 2013 HALO BioClass introduced to bring higher efficiency to proteomics and bioanalytical separations 2014 HALO 2 micron columns designed to deliver 300,000 N/m – higher efficiency than non-core sub-2 micron columns HALO 2 Fused-Core UHPLC Columns Solid Core 1.2 µm 0.4 µm Shell with 90 Å pores 2 µm 2 Higher Plates With Lower Pressure 3 HALO 2 High Pressure Stability Columns:



Mental Health, Healthcare, Public Health, Safety Issues, Medicine, Biochemistry, Molecular Biology, Proteomics, Neuroscience, Molecular Genetics, Glycobiology, Immunology, Pharmacokinetics, Surgery, Living Systems, Biological Systems, Molecular Scale Electronics, Organisms, Ecosystems and other related topics.


Zidane-Audouze-CVetautres 51%

Curriculum  Vitae   ÉTAT  CIVIL     NOM  :


novo1 46%

Each of these genes has no protein-coding homologs in any other genome, but is supported by evidence from expression and, importantly, proteomics data.


celiac disease and autoinmmunity 44%

Different binding motifs of the celiac disease-associated HLA molecules DQ2.5, DQ2.2, and DQ7.5 revealed by relative quantitative proteomics of endogenous peptide repertoires.



Ouandaogo,1,4 Elisa Negroni,1 Virginie Mariot,1 Svetlana Ghimbovschi,2 Brennan Harmon,2 Aurore Wielgosik,1 Camille Loiseau,1,3 Joe Devaney,2 Julie Dumonceaux,1 Gillian Butler-Browne,1 Vincent Mouly,1,* and Ste´phanie Duguez1,* 1Sorbonne Universite ´ s, UPMC University of Paris 06, INSERM UMRS974, CNRS FRE3617, Centre de Recherche en Myologie (CRM), GH Pitie´ ^trie`re, Paris 13, France Salpe Proteomics, and Bioinformatics (GPB) Core of the Intellectual and Developmental Disabilities Research Center (IDDRC), Children’s National Medical Center, Washington, DC 20010, USA 3Sorbonne Universite ´ s, UPMC University of Paris 06, INSERM, UMR-S 1158, Neurophysiologie Respiratoire Expe´rimentale et Clinique, Paris 13, France 4Co-first author *Correspondence:


BACTIBASE a new web-accessible database for bacteriocin 30%

BMC Microbiology BioMed Central Open Access Database BACTIBASE:


EP1694829B1 28%



10.1080@14712598.2017.1378641 26%

The impact of new procedures such as reverse vaccinology, proteomics and plant-based expression of Tb antigens is discussed, as well as their potential contribution in the development of new Tb vaccines.